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Comparison of Stress and Learning Effects of Three Different ...

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HOBFOLL (1989) <strong>of</strong>fered a new theory called the ‘’conservation <strong>of</strong> resources’’ (COR)<br />

theory which is also based on the ‘’psychological stress’’. He furthermore states that the loss<br />

<strong>of</strong> resources is the primary source <strong>of</strong> stress. According to the COR theory, stress occurs in<br />

cases <strong>of</strong> loss or threat <strong>of</strong> resources, or <strong>of</strong> a lack <strong>of</strong> gain following the investment (HOBFOLL<br />

1989, HOBFOLL et al. 1996).<br />

McEWEN <strong>and</strong> WINGFIELD (2003), however, discussed the stress concept within the<br />

framework <strong>of</strong> allostasis <strong>and</strong> defined stress as “events that are threatening to an individual <strong>and</strong><br />

which elicit physiological <strong>and</strong> behavioral responses as a part <strong>of</strong> allostasis in addition to that<br />

imposed by normal life cycle”. In this manner, they introduced two new concepts: allostatic<br />

load, i.e., adaptive responses to daily <strong>and</strong> seasonal individual dem<strong>and</strong>s such as migrating,<br />

breeding, molting etc. <strong>and</strong> allostatic overload, i.e., the state in which the energy requirements<br />

exceed the energy income <strong>of</strong> the individual, or the condition in which the organism continues<br />

to store energy though energy requirements are not exceeded, such as stress related food<br />

consumption.<br />

URSIN <strong>and</strong> ERIKSEN (2004) recently developed a stress theory called the ‘’Cognitive<br />

Activation Theory <strong>of</strong> <strong>Stress</strong>’’ (CATS) based on neurophysiological activation <strong>and</strong> arousal<br />

concepts. According to CATS, the stress response is ‘’an alarm which produces general <strong>and</strong><br />

unspecific neurophysiological activation whenever homeostatic imbalance or threat to<br />

homeostasis <strong>and</strong> life <strong>of</strong> the organism occurs’’.<br />

ERIKSEN et al. (1999) emphasized that the stress response is dynamic <strong>and</strong> develops in phases<br />

<strong>and</strong>, also, that the time course <strong>of</strong> stress response is very important for evaluating relationships<br />

between the stressors <strong>and</strong> the observed physiological responses, as well as for any<br />

pathophysiological consequences <strong>of</strong> such relationships. CATS assumed that ‘’the initial stage<br />

<strong>of</strong> the response-characterized by positive feedback <strong>and</strong> feed-forward mechanism- is followed<br />

by the activation <strong>of</strong> the homeostatic mechanism, <strong>and</strong> subjects with efficient coping show the<br />

fast- <strong>and</strong> short-lasting catecholamine response, while subjects with high defense mechanisms<br />

(related to stimulus expectancies) may show more signs <strong>of</strong> prolonged activation‘’. URSIN <strong>and</strong><br />

ERIKSEN (2004) proposed that when the expectancies, which are attached to the responses,<br />

are positive, there is no health risk in a healthy organism, <strong>and</strong> that the ill-effect only occurs in<br />

case the lack <strong>of</strong> coping.<br />

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